Endothelial Cell Participation in Inflammatory Reaction.
SARS-CoV-2
angiogenesis
endothelial cells
inflammasome
inflammation
thrombosis
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
13 Jun 2021
13 Jun 2021
Historique:
received:
25
04
2021
revised:
08
06
2021
accepted:
11
06
2021
entrez:
2
7
2021
pubmed:
3
7
2021
medline:
8
7
2021
Statut:
epublish
Résumé
Inflammation is an old concept that has started to be considered as an important factor in infection and chronic diseases. The role of leukocytes, the plasmatic components, then of the mediators such as prostaglandins, cytokines, and, in recent decades, of the endothelium has completed the concept of the inflammation process. The function of the endothelium appeared to be crucial as a regulator or the initiator of the inflammatory process. Culture of human endothelial cells and experimental systems made it possible to define the molecular basis of inflammation in vascular diseases, in diabetes mellitus, atherosclerosis, vasculitis and thromboembolic complications. Advanced glycation end product receptor (RAGE), present on endothelial cells (ECs) and monocytes, participates in the activation of these cells in inflammatory conditions. Inflammasome is a cytosolic multiprotein that controls the response to diverse microorganisms. It is positively regulated by stimulator of interferon response CGAMP interactor-1 (STING1). Angiogenesis and thrombotic events are dysregulated during inflammation. ECs appear to be a protector, but also a possible initiator of thrombosis.
Identifiants
pubmed: 34199319
pii: ijms22126341
doi: 10.3390/ijms22126341
pmc: PMC8231964
pii:
doi:
Substances chimiques
Inflammasomes
0
Membrane Proteins
0
Receptor for Advanced Glycation End Products
0
STING1 protein, human
0
Nitric Oxide
31C4KY9ESH
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
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